FDA — authorised 22 April 2021
- Application: BLA761174
- Marketing authorisation holder: GLAXOSMITHKLINE
- Local brand name: JEMPERLI
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised JEMPERLI on 22 April 2021
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 22 April 2021; FDA authorised it on 17 August 2021; FDA has authorised it.
GLAXOSMITHKLINE holds the US marketing authorisation.